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Comparison of MedCem MTA and Formocresol Used in Pulpotomies in Primary Teeth.

H

Hadassah Medical Center

Status

Completed

Conditions

Pulpotomies Primary Teeth
Effectiveness of MedCem MTA® in Pulpotomies Primary Teeth

Treatments

Procedure: MedCem MTA pulpotomies in primary teeth.

Study type

Interventional

Funder types

Other

Identifiers

NCT01962077
Nathalie- HMO-CTIL

Details and patient eligibility

About

assess the effect of MedCem MTA as a pulp medicament following pulpotomy in human primary molars with carious pulp exposure in comparison to Formocresol.

Enrollment

60 patients

Sex

All

Ages

2 to 10 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. healthy children
  2. with Asymptomatic primary molars with a deep carious lesion;
  3. Exposure of a vital pulp by caries;
  4. No clinical or radiographic evidence of pulp degeneration, such as excessive bleeding from the root canal, internal root resorption, inter-radicular and/or periapical bone destruction,swelling, or sinus tract;
  5. Ability to perform a leakage free restoration of the teeth using stainless steel crown, or amalgam/resin based restoration.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 1 patient group

MedCem MTA pulpotomies
Experimental group
Treatment:
Procedure: MedCem MTA pulpotomies in primary teeth.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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